BEUDAMED
    10 results · 26ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    ICS MEDICAL VEMR VIDEO EYE MOVEMENT RECORDER

    FDA 510(k)
    FDA Class 2 ·Neurology

    Arisure Dry Spike

    FDA 510(k)
    FDA Class 2 ·General Hospital

    JBAIDS PLAQUE DETECTION KIT, MODEL JRPD-ASY-0123

    FDA 510(k)
    FDA Class 2 ·Microbiology

    IBP ELBOW INTERLOK FINISH ULNAR COMPONENT STANDARD LEFT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·June 14, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·February 9, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·March 2, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·February 9, 2017

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·February 21, 2013

    LIFEPAK 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·January 19, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·August 1, 2014